Atlas of Genetics and Cytogenetics in Oncology and Haematology


Home   Genes   Leukemias   Solid Tumors   Cancer-Prone   Deep Insight   Case Reports   Journals  Portal   Teaching   

X Y 1 2 3 4 5 6 7 8 9 10 11 12 13 14 15 16 17 18 19 20 21 22 NA

MIR891B (microRNA 891b)

Identity

Alias (NCBI)MIRN891B
HGNC (Hugo) MIR891B
HGNC Alias symbhsa-mir-891b
HGNC Previous nameMIRN891B
LocusID (NCBI) 100126304
Atlas_Id 57395
Location Xq27.3  [Link to chromosome band Xq27]
Location_base_pair Starts at 146001053 and ends at 146001131 bp from pter ( according to hg38-Dec_2013)
Fusion genes
(updated 2017)
Data from Atlas, Mitelman, Cosmic Fusion, Fusion Cancer, TCGA fusion databases with official HUGO symbols (see references in chromosomal bands)

Note

Non-annotated gene. Preliminary data : if you are an author
who wish to write a full paper/card on this gene, go to  How to contribute

DNA/RNA

 



External links

Nomenclature
HGNC (Hugo)MIR891B   33645
Cards
Entrez_Gene (NCBI)MIR891B    microRNA 891b
AliasesMIRN891B
GeneCards (Weizmann)MIR891B
Ensembl hg19 (Hinxton)ENSG00000216064 [Gene_View]
Ensembl hg38 (Hinxton)ENSG00000216064 [Gene_View]  ENSG00000216064 [Sequence]  chrX:146001053-146001131 [Contig_View]  MIR891B [Vega]
ICGC DataPortalENSG00000216064
TCGA cBioPortalMIR891B
AceView (NCBI)MIR891B
Genatlas (Paris)MIR891B
SOURCE (Princeton)MIR891B
Genetics Home Reference (NIH)MIR891B
miRBaseMIR891B
dbDEMCMIR891B
Genomic and cartography
GoldenPath hg38 (UCSC)MIR891B  -     chrX:146001053-146001131 -  Xq27.3   [Description]    (hg38-Dec_2013)
GoldenPath hg19 (UCSC)MIR891B  -     Xq27.3   [Description]    (hg19-Feb_2009)
GoldenPathMIR891B - Xq27.3 [CytoView hg19]  MIR891B - Xq27.3 [CytoView hg38]
ImmunoBaseENSG00000216064
Genome Data Viewer NCBIMIR891B [Mapview hg19]  
Gene and transcription
Genbank (Entrez)-
RefSeq transcript (Entrez)
Consensus coding sequences : CCDS (NCBI)MIR891B
Gene ExpressionMIR891B [ NCBI-GEO ]   MIR891B [ EBI - ARRAY_EXPRESS ]   MIR891B [ SEEK ]   MIR891B [ MEM ]
Gene Expression Viewer (FireBrowse)MIR891B [ Firebrowse - Broad ]
GenevisibleExpression of MIR891B in : [tissues]  [cell-lines]  [cancer]  [perturbations]  
BioGPS (Tissue expression)100126304
GTEX Portal (Tissue expression)MIR891B
Human Protein AtlasENSG00000216064-MIR891B [pathology]   [cell]   [tissue]
Protein : pattern, domain, 3D structure
Domain families : Pfam (Sanger)
Domain families : Pfam (NCBI)
Conserved Domain (NCBI)MIR891B
Human Protein Atlas [tissue]ENSG00000216064-MIR891B [tissue]
Protein Interaction databases
BioGRIDMIR891B
STRING (EMBL)MIR891B
ZODIACMIR891B
Ontologies - Pathways
Litterature
PubMed5 Pubmed reference(s) in Entrez
GeneRIFsGene References Into Functions (Entrez)
EVEXMIR891B
Genes in titleautomatic search in PubMed
REVIEW articlesautomatic search in PubMed
Last year publicationsautomatic search in PubMed

Search in all EBI   NCBI

© Atlas of Genetics and Cytogenetics in Oncology and Haematology
indexed on : Thu Jan 20 12:47:09 CET 2022

Home   Genes   Leukemias   Solid Tumors   Cancer-Prone   Deep Insight   Case Reports   Journals  Portal   Teaching   

For comments and suggestions or contributions, please contact us

jlhuret@AtlasGeneticsOncology.org.